A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5496653



Internal ID273726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18052721..18054590hg38UCSC Ensembl
chr11:18074268..18076137hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381870
hg191870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043664
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5496653
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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